The LUCENT Study - LUng Lesion Assessment Via BF-UCP190F for Central and Extended Nodal Targeting

The Olympus BF-UCP190F bronchoscope combines the reach of a thinner bronchoscope with the benefit of real-time ultrasound, enabling direct lesion visualization and sampling deeper into the lung. Following promising first-in-human data, the LUCENT study aims to evaluate the utility feasibility, effectiveness and safety of this device in a multicenter setting, generating real-world evidence to inform broader adoption in global markets.

NCT Number	NCT07253727
Lead Sponsor	Olympus Europe SE & Co. KG Collaborators: Heidelberg University, Lung Clinic Hemer
Conditions	Bronchoscopy
Enrollment	200 participants
Start Date	2025-12-01
Primary Completion	2027-01-31 (estimated)
Study Completion	2028-08-31 (estimated)
Updated on ClinicalTrials.gov	2025-11-28